Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
2832754 | Molecular Immunology | 2008 | 11 Pages |
Abstract
Human NK cells can be distinguished into CD56bright and CD56dim subsets based on cell surface CD56 density. It has been shown that IL-2 and IL-15 have opposing effects on life and death of CD8+ T cells. However, the roles of IL-2 and IL-15 in regulating these two NK cell subsets remain elusive. In this study, we comparatively analyzed the effects of IL-2 and IL-15 on two NK cell subsets. IL-15 improved the proliferation and activation of CD56dim NK cells in long-term cord blood mononuclear cell culture, but IL-2 only maintained the survival of CD56bright NK cells. The percentage of CD56+Annexin V+ NK cells cultured with IL-15 was lower than that with IL-2; moreover, most of Annexin V+ NK cells were primarily in the CD56dim NK cells. IL-15 cultured NK cells expressed higher level of Bcl-xL than IL-2 cultured cells. Furthermore, IL-15 more strongly upregulated CD25 expression and better maintained the expression of IL-15Rα than IL-2. These results suggest that CD56dim NK cells undergo apoptosis when cultured with IL-2, but IL-15 inhibits their apoptosis and Bcl-xL is associated with the anti-apoptotic effect of IL-15. So IL-15 played a crucial role in sustaining long-lasting functions of CD56dim NK cells.
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Authors
Xiaodong Zheng, Yanyan Wang, Haiming Wei, Bin Ling, Rui Sun, Zhigang Tian,